A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731251



Internal ID154917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16582224..16691148hg38UCSC Ensembl
chr20:16562869..16671793hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38108925
hg19108925
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518224
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731251
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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